ethyl 2-(2,3,5,6-tetrafluoro-4-(3-perfluoroheptyl-1,2,4-oxadiazol-5-yl)phenylamino)acetate

Base Information

Chemical Name:ethyl 2-(2,3,5,6-tetrafluoro-4-(3-perfluoroheptyl-1,2,4-oxadiazol-5-yl)phenylamino)acetate
CAS No.:1370734-22-7
Molecular Formula:C₁₉H₈F₁₉N₃O₃
Molecular Weight:687.26
Hs Code.:

Synonyms:ethyl 2-(2,3,5,6-tetrafluoro-4-(3-perfluoroheptyl-1,2,4-oxadiazol-5-yl)phenylamino)acetate

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Chemical Property of ethyl 2-(2,3,5,6-tetrafluoro-4-(3-perfluoroheptyl-1,2,4-oxadiazol-5-yl)phenylamino)acetate

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Technology Process of ethyl 2-(2,3,5,6-tetrafluoro-4-(3-perfluoroheptyl-1,2,4-oxadiazol-5-yl)phenylamino)acetate

There total 4 articles about ethyl 2-(2,3,5,6-tetrafluoro-4-(3-perfluoroheptyl-1,2,4-oxadiazol-5-yl)phenylamino)acetate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 86.0%

: 919489-99-9
3-pentadecafluoroheptyl-5-pentafluorophenyl-1,2,4-oxadiazole

: 623-33-6
glycine ethyl ester hydrochloride

: 1370734-22-7
ethyl 2-(2,3,5,6-tetrafluoro-4-(3-perfluoroheptyl-1,2,4-oxadiazol-5-yl)phenylamino)acetate

Guidance literature:: With potassium tert-butylate; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1039/c2ob07024c

Reference yield:

: C₁₅H₂F₂₀N₂O₂

: 1370734-22-7
ethyl 2-(2,3,5,6-tetrafluoro-4-(3-perfluoroheptyl-1,2,4-oxadiazol-5-yl)phenylamino)acetate

Guidance literature:: Multi-step reaction with 2 steps

1: 180 °C / Neat (no solvent)

2: potassium tert-butylate / N,N-dimethyl-formamide / 20 °C

With potassium tert-butylate; In N,N-dimethyl-formamide;
DOI:10.1039/c2ob07024c

Reference yield:

: 4314-38-9
pentadecafluoroheptyl amidoxime

: 1370734-22-7
ethyl 2-(2,3,5,6-tetrafluoro-4-(3-perfluoroheptyl-1,2,4-oxadiazol-5-yl)phenylamino)acetate

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / acetone / 20 °C

2: 180 °C / Neat (no solvent)

3: potassium tert-butylate / N,N-dimethyl-formamide / 20 °C

With potassium tert-butylate; potassium carbonate; In N,N-dimethyl-formamide; acetone;
DOI:10.1039/c2ob07024c